Identification and Characterization of the Neisseria gonorrhoeae MscS-Like Mechanosensitive Channel

Infect Immun. 2018 May 22;86(6):e00090-18. doi: 10.1128/IAI.00090-18. Print 2018 Jun.

Abstract

Mechanosensitive channels are ubiquitous in bacteria and provide an essential mechanism to survive sudden exposure to a hypo-osmotic environment by the sensing and release of increased turgor pressure. No mechanosensitive channels have thus far been identified and characterized for the human-specific bacterial pathogen Neisseria gonorrhoeae In this study, we identified and characterized the N. gonorrhoeae MscS-like mechanosensitive channel (Ng-MscS). Electrophysiological analyses by the patch clamp method showed that Ng-MscS is stretch activated and contains pressure-dependent gating properties. Further mutagenesis studies of critical residues forming the hydrophobic vapor lock showed that gain-of-function mutations in Ng-MscS inhibited bacterial growth. Subsequent analysis of the function of Ng-MscS in N. gonorrhoeae by osmotic down-shock assays revealed that the survival of Ng-mscS deletion mutants was significantly reduced compared with that of wild-type strains, while down-shock survival was restored upon the ectopic complementation of mscS Finally, to investigate whether Ng-MscS is important for N. gonorrhoeae during infections, competition assays were performed by using a murine vaginal tract infection model. Ng-mscS deletion mutants were outcompeted by N. gonorrhoeae wild-type strains for colonization and survival in this infection model, highlighting that Ng-MscS contributes to in vivo colonization and survival. Therefore, Ng-MscS might be a promising target for the future development of novel antimicrobials.

Keywords: MscS; Neisseria gonorrhoeae; electrophysiology; gonococcus; host colonization; hypo-osmotic shock; patch clamp.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Escherichia coli
  • Female
  • Gene Expression Regulation, Bacterial
  • Gentamicins / pharmacology
  • HeLa Cells
  • Humans
  • Mechanotransduction, Cellular / genetics
  • Mechanotransduction, Cellular / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Mutagenesis, Site-Directed
  • Mutation
  • Neisseria gonorrhoeae / drug effects
  • Neisseria gonorrhoeae / genetics
  • Neisseria gonorrhoeae / metabolism*
  • Spheroplasts
  • Vagina / microbiology

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Gentamicins